Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

BACKGROUND: Multiple sclerosis (MS) is a complex disorder thought to result from an interaction between environmental and genetic predisposing factors which have not yet been characterised, although it is known to be associated with the HLA region on 6p21.32. Recently, a picture of chronic cerebrosp...

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Detalhes bibliográficos
Main Authors: Ferlini, Alessandra, Bovolenta, Matteo, Neri, Marcella, Gualandi, Francesca, Balboni, Alessandra, Yuryev, Anton, Salvi, Fabrizio, Gemmati, Donato, Liboni, Alberto, Zamboni, Paolo
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2880319/
https://ncbi.nlm.nih.gov/pubmed/20426824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-64
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